Key result
Coxsackievirus A2 infection was identified in 5 of 7,280 children with acute flaccid paralysis, including 3 fully vaccinated children who developed persistent residual paralysis.
Why the study?
The etiological significance of non-polio enteroviruses in acute flaccid paralysis is definitively established only for enteroviruses A71 and D68, leaving the role of other enteroviruses such as Coxsackie A2 unclear.
Observational (n=7,280)
Yes
Coxsackievirus A2 may be an uncommon but potential cause of acute flaccid paralysis resulting in persistent residual paralysis in children.
Coxsackievirus A2 may underlie rare AFP cases with persistent paralysis despite vaccination; hypothesis-generating and requires prospective confirmation.
Surveillance for acute flaccid paralysis syndrome (AFP) in children under 15 is the backbone of the Global Polio Eradication Initiative. Laboratory examination of stool samples from AFP cases allows the detection of, along with polioviruses, a variety of non-polio enteroviruses (NPEV). The etiological significance of these viruses in the occurrence of AFP cases has been definitively established only for enteroviruses A71 and D68. Enterovirus Coxsackie A2 (CVA2) is most often associated with vesicular pharyngitis and hand, foot and mouth disease. Among 7280 AFP cases registered in Russia over 20 years (2001-2020), CVA2 was isolated only from five cases. However, these included three children aged 3 to 4 years, without overt immune deficiency, immunized with 4-5 doses of poliovirus vaccine in accordance with the National Vaccination Schedule. The disease resulted in persistent residual paralysis. Clinical and laboratory data corresponded to poliomyelitis developing during poliovirus infection. These findings are compatible with CVA2 being the cause of AFP. Molecular analysis of CVA2 from these patients and a number of AFP cases in other countries did not reveal association with a specific phylogenetic group, suggesting that virus genetics is unlikely to explain the pathogenic profile. The overall results highlight the value of AFP surveillance not just for polio control but for studies of uncommon AFP agents.
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Ivanova et al. (2022) conducted an observational in Acute flaccid paralysis syndrome (AFP) (n=7,280). Coxsackievirus A2 (CVA2) infection was evaluated on Isolation of Coxsackievirus A2 and development of persistent residual paralysis. Coxsackievirus A2 infection was identified in 5 of 7,280 children with acute flaccid paralysis, including 3 fully vaccinated children who developed persistent residual paralysis.
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